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[人宫颈癌细胞系耐药逆转的研究]

[Study on the reversion of drug resistance in human cervical cancer cell lines].

作者信息

Chen H, Chen H, Wu X

机构信息

Department of Obstetrics and Gynecology, Zhongnan Hospital, Wuhan University, Wuhan 430071, China.

出版信息

Zhonghua Fu Chan Ke Za Zhi. 2001 Nov;36(11):669-71.

Abstract

OBJECTIVE

To determine the resistance reversion of mitomycin (MMC) by 3'-Keto-bmt1-val2-cyclosporin (SDZ PSC 833) in human cervical cancer in vitro and in vivo. METHEDS: A xenografted mitomycin resistant mice model of cervical cancer was devolped. The reversion of mitomycin resistance by SDZ PSC 833 (1 or 3 mg/L) was detected from human cervical cancer cell (Hela) and its resistant subline Hela/MMC in vitro and in vivo. Studies in vitro include drug resistance reversion experiment and the changes of morphology. Studies in vivo including tumor volume and tumor related histopathological changes in the autopsied specimen were evaluated by comparing random sections of each group.

RESULTS

Nontoxic doses of SDZ PSC 833 could result in almost partial reversion of MMC-resistance of Hela/MMC. In vivo studies also showed SDZ PSC 833 augmented the growth inhibitory effect of mitomycin on Hela/MMC xenografted in nude mice.

CONCLUSION

SDZ PSC 833 can overcome mitomycin resistance of Hela/MMC in vitro and in vivo, so SDZ PSC 833 will be a better candidate clinically for reversing multidrug resistance.

摘要

目的

在体外和体内确定3'-酮基-bmt1-缬氨酸2-环孢菌素(SDZ PSC 833)对人宫颈癌丝裂霉素(MMC)耐药性的逆转作用。方法:建立宫颈癌丝裂霉素耐药异种移植小鼠模型。检测SDZ PSC 833(1或3 mg/L)在体外和体内对人宫颈癌细胞(Hela)及其耐药亚系Hela/MMC丝裂霉素耐药性的逆转情况。体外研究包括耐药逆转实验和形态学变化。体内研究通过比较每组随机切片评估尸检标本中的肿瘤体积和肿瘤相关组织病理学变化。结果:无毒剂量的SDZ PSC 833可导致Hela/MMC对MMC的耐药性几乎部分逆转。体内研究还表明,SDZ PSC 833增强了丝裂霉素对裸鼠体内移植的Hela/MMC的生长抑制作用。结论:SDZ PSC 833在体外和体内均可克服Hela/MMC对丝裂霉素的耐药性,因此SDZ PSC 833在临床上将是逆转多药耐药性的更好候选药物。

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